1. Academic Validation
  2. Endothelial Myosin IIA Is Required for the Maintenance of Blood-Brain Barrier Integrity

Endothelial Myosin IIA Is Required for the Maintenance of Blood-Brain Barrier Integrity

  • Cells. 2024 Oct 1;13(19):1635. doi: 10.3390/cells13191635.
Yanan Deng 1 Ziqi Qiao 1 Changping Zhou 1 Yujun Pei 1 Han Xu 1 Xuya Kang 1 Jincai Luo 1 2
Affiliations

Affiliations

  • 1 Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, School of Future Technology, Peking University, Beijing 100871, China.
  • 2 College of Future Technology, Peking University, Beijing 100871, China.
Abstract

Brain endothelial cells (ECs) are essential elements of the blood-brain barrier (BBB), maintaining its integrity through both paracellular junctions and transcellular transport systems. Myosin IIA, a multifunctional protein, plays a significant role in various cellular processes, including cytoskeletal maintenance, cell division, and signal transduction. While Myosin IIA has been implicated in bleeding and ischemic stroke, its role in regulating BBB integrity under physiological conditions remains unclear. In this study, we investigated the impact of Myosin IIA deficiency on BBB integrity using intravenous tracer injections and models of epilepsy. Flow cytometry, Western blot, and Real-Time PCR were employed to isolate brain cells and assess changes in protein and mRNA levels. Additionally, immunofluorescence staining and electron microscopy were used to explore alterations in protein expression and the structure of BBB. Our results demonstrate that endothelial Myosin IIA deficiency increased BBB permeability and exacerbated symptoms in BBB-related diseases. Mechanistically, we found that Myosin IIA modulates β-catenin transcription and protein interactions. The overexpression of β-catenin in brain endothelial Myosin IIA deficiency mice improved BBB integrity and reduced disease severity. This study establishes Myosin IIA as a critical regulator of BBB integrity and suggests new therapeutic targets for vascular diseases.

Keywords

adhesion molecules; animal models; blood–brain barrier; endothelium; vascular biology.

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